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sigven · Nov 14, 2017 · 3d6ed3c · 3d6ed3c
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diff --git a/docs/_build/doctrees/annotation_resources.doctree b/docs/_build/doctrees/annotation_resources.doctree
diff --git a/docs/_build/doctrees/environment.pickle b/docs/_build/doctrees/environment.pickle
diff --git a/docs/_build/html/_sources/annotation_resources.rst.txt b/docs/_build/html/_sources/annotation_resources.rst.txt
@@ -21,9 +21,6 @@ Variant frequency databases
 ~~~~~~~~~~~~~~~~~~~~~~~~~~~
 
 -  *COSMIC - Deprecated in 0.5.0 due to COSMIC licensing restrictions*
--  `ICGC v23 <https://dcc.icgc.org/>`__ - Somatic mutations discovered
-   in all ICGC (International Cancer Genomics Consortium) tumor cohorts
-   (Dec 2016)
 -  `gnomAD r1 <http://exac.broadinstitute.org/>`__ - germline variant
    frequencies exome-wide (March 2017)
 -  `dbSNP b147 <http://www.ncbi.nlm.nih.gov/SNP/>`__ - database of short

diff --git a/docs/_build/html/annotation_resources.html b/docs/_build/html/annotation_resources.html
@@ -174,9 +174,6 @@ <h2><em>Insilico</em> predictions of effect of coding variants<a class="headerli
 <h2>Variant frequency databases<a class="headerlink" href="#variant-frequency-databases" title="Permalink to this headline">¶</a></h2>
 <ul class="simple">
 <li><em>COSMIC - Deprecated in 0.5.0 due to COSMIC licensing restrictions</em></li>
-<li><a class="reference external" href="https://dcc.icgc.org/">ICGC v23</a> - Somatic mutations discovered
-in all ICGC (International Cancer Genomics Consortium) tumor cohorts
-(Dec 2016)</li>
 <li><a class="reference external" href="http://exac.broadinstitute.org/">gnomAD r1</a> - germline variant
 frequencies exome-wide (March 2017)</li>
 <li><a class="reference external" href="http://www.ncbi.nlm.nih.gov/SNP/">dbSNP b147</a> - database of short

diff --git a/docs/_build/html/searchindex.js b/docs/_build/html/searchindex.js
diff --git a/docs/annotation_resources.md b/docs/annotation_resources.md
@@ -9,7 +9,6 @@
 
 ###  Variant frequency databases
   * *COSMIC - Deprecated in 0.5.0 due to COSMIC licensing restrictions*
-  * [ICGC v23](https://dcc.icgc.org/) - Somatic mutations discovered in all ICGC (International Cancer Genomics Consortium) tumor cohorts (Dec 2016)
   * [gnomAD r1](http://exac.broadinstitute.org/) - germline variant frequencies exome-wide (March 2017)
   * [dbSNP b147](http://www.ncbi.nlm.nih.gov/SNP/) - database of short genetic variants (April 2016)
   * [1000Genomes phase3](ftp://ftp.1000genomes.ebi.ac.uk/vol1/ftp/release/20130502/) - germline variant frequencies genome-wide (May 2013)

diff --git a/docs/annotation_resources.rst b/docs/annotation_resources.rst
@@ -21,9 +21,6 @@ Variant frequency databases
 ~~~~~~~~~~~~~~~~~~~~~~~~~~~
 
 -  *COSMIC - Deprecated in 0.5.0 due to COSMIC licensing restrictions*
--  `ICGC v23 <https://dcc.icgc.org/>`__ - Somatic mutations discovered
-   in all ICGC (International Cancer Genomics Consortium) tumor cohorts
-   (Dec 2016)
 -  `gnomAD r1 <http://exac.broadinstitute.org/>`__ - germline variant
    frequencies exome-wide (March 2017)
 -  `dbSNP b147 <http://www.ncbi.nlm.nih.gov/SNP/>`__ - database of short